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Completed Phase 3 Interventional Results available

A Clinical Trial to Evaluate the Efficacy and Safety of Testosterone Gel in Adult Hypogonadal Males

ClinicalTrials.gov ID: NCT02149264

Public ClinicalTrials.gov record NCT02149264. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 7:32 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Open-Label, Non-Randomized, Clinical Trial to Evaluate the Efficacy and Safety of FE 999303 (Testosterone Gel) in Adult Hypogonadal Males

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 3, open-label, non-randomized, clinical trial to evaluate the efficacy and safety of FE 999303 (Testosterone gel) in adult hypogonadal males.

Study identification

NCT ID
NCT02149264
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
160 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2014 (Type not available)
Primary completion
May 2015 (Actual)
Completion
Jun 2015 (Actual)
Last update posted
Oct 26, 2017

2014 – 2015

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
Investigational site Anniston Alabama — —
Investigational site Huntsville Alabama — —
Investigational site Newport Beach California — —
Investigational site Denver Colorado — —
Investigational site New Haven Connecticut — —
Investigational site Aventura Florida — —
Investigational site Clearwater Florida — —
Investigational site Mishawaka Indiana — —
Investigational site Watertown Massachusetts — —
Investigational site Troy Michigan — —
Investigational site Edison New Jersey — —
Investigational site Lawrence New Jersey — —
Investigational site Garden City New York — —
Investigational site New York New York — —
Investigational site Poughkeepsie New York — —
Investigational site Purchase New York — —
Investigational site Bala-Cynwyd Pennsylvania — —
Investigational site Warwick Rhode Island — —
Investigational site Mt. Pleasant South Carolina — —
Investigational site Nashville Tennessee — —
Investigational site Webster Texas — —
Investigational site Norfolk Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02149264, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 26, 2017 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02149264 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →